At Tata Elxsi, our team specializes in Post Market Surveillance, ensuring medical devices meet stringent international standards. With a background in Biomedical Engineering from Dhanalakshmi Srinivasan Engineering College, my focus is on analyzing clinical trial data and managing risks to maintain compliance with EU MDR, FDA, and Health Canada regulations.Recently, we spearheaded a pilot project, navigating Post Market Surveillance activities with precision. My commitment is to further innovation in medical device regulation, leveraging my clinical trials expertise to contribute to the safety and efficacy of healthcare solutions.